Developing a new generation of tests for genotyping hemophilia-causative rearrangements involving int22h and int1h hotspots in the factor VIII gene

Journal of Thrombosis and Haemostasis

Volumn 6, Issue 5, 2008, Pages 830-836

  Rossetti, Liliana C ^a   Radic, C P ^a   Larripa, I B ^a   De Brasi, C D ^a  

^a INST DE INVEST HEMATOLOGICAS   (Argentina)

Author keywords

F8 inversions; Hemophilia A; Inverse shifting PCR

Indexed keywords

BLOOD CLOTTING FACTOR 8;

ARTICLE; CHROMOSOME INVERSION; CONTROLLED STUDY; DIAGNOSTIC TEST; DIAGNOSTIC VALUE; FEMALE; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENOTYPE; HEMOPHILIA A; HUMAN; INTRON; INVERSE POLYMERASE CHAIN REACTION; INVERSE SHIFTING POLYMERASE CHAIN REACTION; MAJOR CLINICAL STUDY; MALE; MOSAICISM; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PATTERN RECOGNITION; PRIORITY JOURNAL; TASK PERFORMANCE; VALIDATION STUDY;

DNA MUTATIONAL ANALYSIS; FACTOR VIII; GENE REARRANGEMENT; GENOTYPE; HEMOPHILIA A; HUMANS; INVERSION, CHROMOSOME; POLYMERASE CHAIN REACTION;

EID: 42149170507     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1111/j.1538-7836.2008.02926.x     Document Type: Article

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